510(k) K163673 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
Fortilink-C with TETRAfuse 3D Technology
| Applicant | Rti Surgical, Inc., Alachua FL, US |
| Decision | Substantially Equivalent, May 23, 2017 |
| Received | Dec 27, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163673
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.